10 ott - Milano
Iqvia
Overview
In this role you lead strategic delivery of global clinical trials, partnering with sponsors and cross-functional teams to accelerate development of innovative therapies. You guide multi-regional studies, ensuring quality, timelines and budget alignment while navigating regulatory requirements. You work with senior sponsors to provide strategic solutions and shape study outcomes. This role offers broad global exposure, leadership impact, and the chance to advance patient outcomes through cutting-edge research.
Responsabilità
- Lead delivery of complex global and multi-regional clinical studies, ensuring operational excellence
- Act as primary strategic partner for sponsors, offering leadership and innovative solutions
- Provide direction to cross-functional regional teams to drive collaboration and accountability
- Oversee study timelines, budgets, quality, risks, and financial performance
- Drive proactive risk management, issue resolution, and stakeholder alignment
- Ensure studies comply with ICH-GCP,
regulatory requirements, and contractual commitments
Requisiti fondamentali
- Bachelor's degree in Life Sciences or related discipline
- 7+ years of clinical research experience with global or multi-regional trials in CRO/pharma/biotech
- Experience leading renal, obesity and/or MASH global studies preferred
- Strong knowledge of clinical trial conduct, ICH-GCP, and regulatory requirements
- Proven success in leading cross-functional teams and managing study delivery (timelines, budgets, quality, risks)
- Ability to build trusted sponsor relationships and manage senior stakeholders
- Excellent leadership, communication, problem-solving, and decision-making skills
- Passion for advancing clinical research and patient outcomes
- leadership
- communication
- problem-solving
- ICH-GCP compliance
- regulatory knowledge
- study delivery management
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